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DAVID PETILLO, M.D.
M.D.
Internal Medicine Physician
NPI: 1285669614IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine Physician
Emergency Medicine
Code: 207P00000X
72186(MA)
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
72186(MA)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
GEORGETOWN UNIVERSITY SCHOOL OF MEDICINE
Class of 1983
Research & Publications (20)
Genome-wide scan identifies novel modifier loci of acromegalic phenotypes for isolated familial somatotropinoma.
PMID 19443539·Endocr Relat Cancer·2009
8-other
A comparison study reveals important features of agreement and disagreement between summarized DNA and RNA data obtained from renal cell carcinoma.
PMID 18790077·Mutat Res·2008
4-observational
Somatic pairing of chromosome 19 in renal oncocytoma is associated with deregulated EGLN2-mediated [corrected] oxygen-sensing response.
PMID 18773095·PLoS Genet·2008
8-other
Identification of copy number alterations and its association with pathological features in clear cell and papillary RCC.
PMID 18682315·Cancer Lett·2008
8-other
Deficiency of FLCN in mouse kidney led to development of polycystic kidneys and renal neoplasia.
PMID 18974783·PLoS One·2008
7-preclinical
Renal translocation carcinomas: clinicopathologic, immunohistochemical, and gene expression profiling analysis of 31 cases with a review of the literature.
PMID 18344867·Am J Surg Pathol·2008
5-case
Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms.
PMID 18285835·Eur J Hum Genet·2008
8-other
Combining differential expression, chromosomal and pathway analyses for the molecular characterization of renal cell carcinoma.
PMID 18542781·Can Urol Assoc J·2007
8-other
Preparing the "soil": the primary tumor induces vasculature reorganization in the sentinel lymph node before the arrival of metastatic cancer cells.
PMID 17062557·Cancer Res·2006
7-preclinical
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046109·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046107·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046105·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046102·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046098·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046094·Hum Genet·2004
8-other
Human gene mutations. Gene symbol: HRPT2. Disease: Hyperparathyroidism Jaw-tumor syndrome.
PMID 15046050·Hum Genet·2004
8-other
Germline and de novo mutations in the HRPT2 tumour suppressor gene in familial isolated hyperparathyroidism (FIHP).
PMID 14985403·J Med Genet·2004
8-other
The t(1;3) breakpoint-spanning genes LSAMP and NORE1 are involved in clear cell renal cell carcinomas.
PMID 14667507·Cancer Cell·2003
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 111 GROSSMAN DR
BRAINTREE, MA 02184 - Phone
- (781) 849-1000
Quick Facts
- NPI
- 1285669614
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 43
- Publications
- 20
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